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临床试验/NCT01713504
NCT01713504已完成不适用

Identification of New Markers in the Hypereosinophilic Syndrome

University Hospital, Lille2 个研究点 分布在 1 个国家目标入组 41 人开始时间: 2010年6月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
41
试验地点
2
主要终点
The aim is to characterize, through an approach immunoprotéomique, new HES biomarkers more informative and easier access than those currently available to us. These biomarkers will help to the diagnosis of HES, compared with other causes of eosinophilia.

研究概览

简要总结

The purpose is to characterize new hypereosinophilic syndrome biomarkers more informative and more accessible compared to those that we have already thanks to a proteomic approach. This will help the investigators to diagnose the this disease.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • dated and signed informed consent
  • virale serology negative or negative result less than 6 months
  • virale serology negative for HBV or vaccinated patient
  • virale serology negative or negative result less than 6 months
  • negative pregnancy test or female menopause for at least 1 year

排除标准

  • subject enable adult, under guardianship or under protective measures of justice
  • Refusal or inability to give informed consent
  • The hypereosinophilic syndrome explained origin other than than atopy, bullous pemphigoid, the Churg-Strauss syndrome and DRESS

研究组 & 干预措施

Hypereosinophilic syndrome unexplained

Experimental

干预措施: biologie sample (Biological)

Hypereosinophilic syndrome explained

Active Comparator

干预措施: biologie sample (Biological)

Normal rate of eosinophilic

Sham Comparator

干预措施: biologie sample (Biological)

结局指标

主要结局

The aim is to characterize, through an approach immunoprotéomique, new HES biomarkers more informative and easier access than those currently available to us. These biomarkers will help to the diagnosis of HES, compared with other causes of eosinophilia.

时间窗: one month after patient inclusion

次要结局

未报告次要终点

研究者

发起方
University Hospital, Lille
申办方类型
Other
责任方
Sponsor

研究点 (2)

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